Knowledge of all 8 competency domains is expected and experience within applicable domains specific to unit
needs.
- Scientific Concepts and Research Design
- Ethical Participant Safety Considerations
- Investigational Products Development and Regulation
- Clinical Study Operations (GCPs)
- Study and Site Management
- Data Management and Informatics
- Leadership and Professionalism
- Communication and Teamwork
This position may independently provide study coordination for simple and moderately complex clinical research studies. As a member of a coordination team, this position may help support a portfolio of projects with varying levels of complexity.
Additional duties include:
- Collects and maintains Pediatric Neurocritical Care database.
- Screens and oversees the recruitment of subjects, coordinates the scheduling of experiments and the collection, processing and analysis of data and monitors subjects. Studies include IPSS, Ped- QuEST, and BOOST-3 enrollment,
- Oversees IRB preparation and submission for studies, and for patient consenting and enrollment.
- Collaborates with Neurocritical Care faculty, support teams, and stakeholders to ensure the development and implementation of consistent system standards. Uses existing procedures to solve routine or standard problems.